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临床试验/IRCT2017082935979N1
IRCT2017082935979N1已完成2 期

Comparing the analgesic effect of intrathecal Sufentanil with intravenous Acetaminophen in combination with low-dose ketamine onl abor pain

Vice chancellor for research in Qazvin university of medical sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
no limit 至 no limit(—)
性别
Female

入选标准

  • Inclusion criteria are as follows:
  • oPregnant women who are candidates for natural delivery and are in the active phase (Cervical dilatation of 5-3 cm);
  • oPregnant women with no history of physical and psychological illness or biochemical abnormalities (ASA I class);
  • oPregnant women who have written and complete consent for the study.
  • Exclusion criteria are as follows:
  • oDissatisfaction pregnant women;
  • oMother's preeclampsia and eclampsia;
  • oInsulin-dependent diabetes;
  • oMother drug abuse history;
  • oUsing any analgesic method before entering the study;
  • oHistory of liver disease;
  • oHistory or presence of bleeding disorder and coagulation disorders in the mother;
  • ousing anticoagulant drugs;
  • oHistory of mental illness or using antidepressants or anticonvulsants;
  • oAny contraindication for spinal anesthesia;
  • oHistory of allergic reactions or intolerant to the drugs studied (Sufentanil, acetaminophen and ketamine);
  • oAny significant or severe systemic disease that limits usual and natural activities (such as kidney disease that require dialysis, class 2 heart failure and ….).

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research in Qazvin university of medical sciences

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